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Diss Factsheets
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EC number: 939-516-4 | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- Not stated
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted prior to test guidelines and GLP.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 967
- Report date:
- 1967
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- Rats were exposed to vapors generated from test material heated at 200C. Exposure time ranged from 1 to 7 hours
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Glycerol
- EC Number:
- 200-289-5
- EC Name:
- Glycerol
- Cas Number:
- 56-81-5
- Molecular formula:
- C3H8O3
- IUPAC Name:
- glycerol
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): Glycerine
- Substance type: not specified in the report
- Physical state: not specified in the report
- Analytical purity: not specified in the report
- Impurities (identity and concentrations): not specified in the report
- Composition of test material, percentage of components:not specified in the report
- Isomers composition: not specified in the report
- Purity test date: not specified in the report
- Lot/batch No.: not specified in the report
- Expiration date of the lot/batch: not specified in the report
- Stability under test conditions: not specified in the report
- Storage condition of test material: not specified in the report
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- No additional information available.
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on inhalation exposure:
- Saturated vapor atmosphere generated by passing compressed air throught the test material contained in a fritter-finger glass bubbler immersed in an oil bath heated tp approximately 200°C and introduced into the exposure chamber. For the L(Ct)50 experiment, the same vapor was mixed with room air (1:1) before introduction into the exposure chamber.
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- >= 1 - <= 7 h
- Concentrations:
- Nominal concentration 11.0 mg/L
- No. of animals per sex per dose:
- Groups of 5 rats were exposed for 1, 2 and a maximum of 7 hours.
- Control animals:
- not specified
- Details on study design:
- No additional information available.
- Statistics:
- No additional information available.
Results and discussion
- Preliminary study:
- Not applicable.
Effect levels
- Sex:
- male
- Dose descriptor:
- other: L(Ct)50
- Effect level:
- 4 655 other: mg-min/liter
- Based on:
- test mat.
- Exp. duration:
- 7 h
- Mortality:
- See below.
- Clinical signs:
- other: No additional information available.
- Body weight:
- No additional information available.
- Gross pathology:
- See below.
- Other findings:
- No additional information available.
Any other information on results incl. tables
In a preliminary study, no mortality was observed in rats exposed to a saturated vapor for 1 hour and all animals died within 48 hours after exposure to a saturated vapor for 2 hours.
In the L(Ct)50 experiments, compressed air at the rate of 500 ml/minute was bubbled through glycerine which was heated to 200C. The rate of vaporization of glycerine under these conditions, was gravimetrically determined and calculated to be 11.0 mg/minute. The vapor-laden air was diluted by adding make-up air at the rate of 500 ml/minute. The total airflow (volume of air emerged from heated compound plus the volume of make-up air added per unit time), entering the exposure chamber was 1 liter/minute. The nominal concentration of glycerine in the experimental atmosphere was therefore 11.0 mg/L.
During the initial four hours of exposure, no significant adverse effect was observed. However, after approximately 240 minutes, signs of mild irritation, indicated by hyperemia of the eyelids and nasal discharges were observed. These conditions became more severe as the exposure progressed. The animals eventually salivated profusely and exhibited dyspneic respiratory patterns. After approximately 360 minutes, all animals began gasping for air and lay in prostration. Two animals died at approximately the 419 minute timepoint. The third one died shortly after the termination of the exposure. The fourth animal succumbed at approximately 30 minutes post-exposure. The remaining animal succumbed on the fourth post-exposure day. Based upon the time-to-death data, an approximate Lt50 was graphically determined to be 423 minutes.
The L(Ct)50 was obtained by multiplying the nominal chamber concentration, C, with the estimated Lt50 and was equal to 4655 mg-min/liter.
Necropsies of the animals which succumbed revealed: 1) desquamation of the epithelium of the trachea, 2) hyperemia and slight edema of the lung tissues, and 3) extreme distention of the stomach and intestines with air. No significant gross pathological condition was detected in other organs or tissues.
Applicant's summary and conclusion
- Interpretation of results:
- Category 5 based on GHS criteria
- Remarks:
- Migrated information
- Conclusions:
- Under the conditions of the study, the acute inhalation exposure of rats for two hours to saturated vapors generated at 200°C produced 100 per cent mortality, while for exposures of one hour, no mortality was observed. The nominal concentration was 11 mg/L and this study is of a condensation aerosol. Thus the 1 hour LC50 based on nominal concentration was >11 mg/L. Under the OECD GHS guidelines, a 4 hr LC50 can be determined from a 1 hour LC50 by dividing by 4. Thus a calculated 4 hour LC50 value based on nominal concentration would be >2.75 mg/L.
- Executive summary:
The acute toxicity following 1 or 2 hours exposure to saturated vapors of glycerine (generated by passing air through test material heated to 200C) was determined. Under the conditions of the study, the acute inhalation exposure of rats for two hours to saturated vapors generated at 200°C produced 100 per cent mortality, while for exposures of one hour, no mortality was observed. The nominal concentration was 11.0 mg/L and this study is of a condensation aerosol. Thus the 1 hour LC50 based on nominal concentration was >11.0 mg/L. Under the OECD GHS guidelines, a 4 hr LC50 can be determined from a 1 hour LC50 by dividing by 4. Thus a calculated 4 hour LC50 value based on nominal concentration would be >2.75 mg/L.
In addition the L(Ct)50 was determined following exposure to 1100 mg/L. The L(Ct)50 for Glycerine was 4655 mg minute/liter.
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